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ONTOLOGY REPORT - ANNOTATIONS


Term:hypotrichosis 7
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Accession:DOID:0110704 term browser browse the term
Definition:A hypotrichosis that has_material_basis_in a autosomal recessive mutation of LIPH on chromosome 3q27.2. (DO)
Synonyms:exact_synonym: HYPT7;   Hypotrichosis, Autosomal Recessive;   Hypotrichosis, Localized, Autosomal Recessive, 2;   LAH2;   Mari type Alopecia universalis congenita;   Total Hypotrichosis, Mari Type
 primary_id: MESH:C536973
 alt_id: DOID:9000861;   OMIM:604379;   RDO:0002708;   RDO:9003979
For additional species annotation, visit the Alliance of Genome Resources.


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hypotrichosis 7 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Liph lipase H JBrowse link 11 82,680,167 82,732,145 RGD:8554872
RGD:7240710

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  disease 14759
    Developmental Diseases 7628
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 6666
        genetic disease 5913
          hypotrichosis 7 1
Path 2
Term Annotations click to browse term
  disease 14759
    disease of anatomical entity 13978
      nervous system disease 9097
        sensory system disease 4231
          skin disease 2240
            hair disease 201
              hypotrichosis 93
                alopecia 74
                  hypotrichosis 7 1
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